Results 51 to 60 of about 4,786 (283)
Dental implants in patients with oral mucosal alterations : an update [PDF]
, 2011 Objective: To determine whether a series of diseases of the oral mucosa - Sjögren syndrome, ectodermal dysplasia, epidermolysis bullosa and lichen planus - reduce the survival rate of dental implants. Material and Method: A Medline search was carried out
Ata-Ali Mahmud, Francisco Javier +4 more
core +1 more source
European Journal of Special Education ResearchAim: The purpose of the case report was to highlight the clinical features and multidisciplinary approach to managing children suffering from Christ-Siemens-Touraine syndrome with complete anodontia and its prosthetic rehabilitation.
Manesh Lahori +5 more
semanticscholar +1 more source
Contemporary Clinical Dentistry, 2011 Solitary median maxillary central incisor (SMMCI) is a rare dental anomaly. It is estimated to occur in 1:50,000 live births. The SMMCI tooth differs from the normal central incisor in that the crown form is symmetric and it develops and erupts precisely
Ashok Utreja +2 more
doaj +1 more source
Checklist of the Invertebrate Animals Reported from the Region of Port Aransas, Texas [PDF]
, 1960 This checklist is of preliminary form with the hope that this will be a beginning for a more complete annotated list of the fauna and flora of this region. In many cases this list is quite obviously incomplete, however further work on the taxonomy of
Trott, Lamarr B.
core +1 more source
USE OF DIGITAL TECHNOLOGY IN THE REHABILITATION OF PATIENTS WITH PRIMARY ANODONTIA
The Bulletin of Contemporary Clinical Medicine. Introduction. Number of patients with hypodontia has increased at orthodontic appointments. According to different authors, the frequency of tooth rudiments absence ranges from 2 % to 16.5 %.
Louise I. Nikitina +2 more
semanticscholar +1 more source
X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle
Genetics Selection Evolution, 2003 Ectodermal dysplasias are a large group of rare genetic disorders characterized by impaired development of hair, teeth, and eccrine glands in humans, mice, and cattle.
Drögemüller Cord +2 more
doaj +1 more source
Prosthetic rehabilitation of a young patient with Hypophosphatasia - A review and case report
Contemporary Clinical Dentistry, 2012 Hypophosphatasia is a congenital disease characterized by deficiency of serum and tissue non-specific alkaline phosphatase activity. The disease occurs due to mutations in the liver/bone/kidney alkaline phosphatase gene.
Partapjot S Grewal, Kanu Priya Gupta
doaj +1 more source
Familial cases of missing mandibular incisor: three case presentations [PDF]
, 1999 Hypodontia is the congenital absence of one or more teeth because of agenesis. The most commonly missing teeth are the third molars, the maxillary lateral incisors and the second premolars.
Ngeow, Dr. W.C.
core
Orthodontics &Craniofacial Research, EarlyView.ABSTRACT Crouzon and Apert syndromes are rare syndromic craniosynostoses frequently associated with craniofacial and dental anomalies, including tooth agenesis. Although individual studies have reported tooth agenesis prevalence data in specific populations, no attempts have been made to systematically synthesise these data.
M. Cecilia Becerril Santos +3 more
wiley +1 more source
Dental agenesis in cleft lip and/or palate pf the “Centro Pró-Sorriso” – Universidade José do Rosário Vellano [PDF]
RGO: Revista Gaúcha de Odontologia, 2008 Objective: Analyze periapical and panoramic radiographs in order to define the incidence of dental agenesis in carriers of cleft lip and/or cleft palate among patients of UNIFENAS “Centro Pró-Sorriso” (Pro-Smile Center) in Alfenas – MG.
Orivaldo Tavano +1 more
doaj